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Brain & Development|December 12, 2001
Mind and brain in Rett disorderA M Kerr, P Belichenko, T Woodcock, et al.Journal of Medical Genetics|September 13, 2005
Lost in translation: translational interference from a recurrent mutation in exon 1 of MECP2A Saxena, D de Lagarde, H Leonard, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2000
Rett syndrome: critical examination of clinical features, serial EEG and video-monitoring in understanding and managementR A Cooper, A M Kerr, P M AmosNeuropediatrics|April 1, 1995
Short fourth toes in Rett syndrome: a biological indicatorA M Kerr, J M Mitchell, P E RobertsonPlos One|November 2, 2018
Correction: Adding insult to injury: Ship groundings are associated with coral disease in a pristine reefL J Raymundo, W Y Licuanan, A M KerrPlos One|September 13, 2018
Adding insult to injury: Ship groundings are associated with coral disease in a pristine reefL J Raymundo, W Y Licuanan, A M KerrBritish Journal of Haematology|September 1, 2001
HFE mutations, iron deficiency and overload in 10,500 blood donorsH A Jackson, K Carter, C Darke, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2000
Abnormalities in urinary pterin levels in Rett syndromeS Messahel, A E Pheasant, H Pall, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2004
Population based study of late onset cerebellar ataxia in south east WalesM B Muzaimi, J Thomas, S Palmer-Smith, et al.American Journal of Human Genetics|September 1, 1993
Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosityG Chenevix-Trench, C Wicking, J Berkman, et al.Pageof 8